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WorksheetsRates equilibrium Hess' Law
Total questions: 27
Worksheet time: 26mins
Using the equations below:
C(s) + O2(g) → CO2(g) ∆H = –390 kJ
Mn(s) + O2(g) → MnO2(s) ∆H = –520 kJ
what is ∆H (in kJ) for the following reaction?
MnO2(s) + C(s) → Mn(s) + CO2(g)
910
130
-130
-910
For Hess' Law to be used what must be the same for all of the reactions being studied?
The initial conditions of pressure and temperature.
The final conditions of pressure and temperature.
The initial and the final conditions of pressure and temperature.
The initial and the final conditions of pressure and temperature, and the number of moles of reactants.
Which of the following statements are true for the reaction:
SO2(g) + 1/2O2(g) ↔ SO3(g) ΔH = –92 kJ mol-1
Where ↔ indicates that the reaction can proceed in the forward and the reverse direction.
The forward and reverse reaction both produce 92 kJ of energy.
Oxidising 2 moles of SO2 would produce twice as much energy.
The reverse reaction has an enthalpy of +92 kJ mol-1.
Collecting the SO3 produced in the liquid state would not change the measured enthalpy.
In order to find the enthalpy of combustion of C3H8 how must the enthalpy changes be arranged?
ΔH3 = ΔH1 + ΔH2
ΔH2 = ΔH3 - ΔH1
ΔH1 = ΔH2 - ΔH3
0 = ΔH1 + ΔH2 + ΔH3
Standard conditions are defined as...
298K and 1.00 x 105 kPa
273K and 1.00 x 105 kPa
C(s) + O2(g) -> CO2(g) ∆H=a
H2(g) + ½O2(g) -> H2O(l) ∆H=b
C4H9OH(l) + 6O2(g) -> 4CO2(g) + 5H2O(l) ∆H=c
What is the enthalpy change for the reaction shown below?
4C(g) + 5H2(l) + ½O2(g) -> C4H9OH(l)
C(s, graphite) + 1⁄2O2(g) --> CO(g) cannot be measured directly since some carbon dioxide is always formed in the reaction.
It can be calculated using Hess’s Law and the enthalpy changes of combustion of graphite and of carbon monoxide.
C(s, graphite) + O2(g) --> CO2 ΔH=-394 kJmol–1
CO(g) + 1⁄2O2(g) --> CO2 ΔH=-283 kJmol–1
The enthalpy change for the reaction of graphite with oxygen to give carbon monoxide is
How much energy is associated with the process of creating 4 mol NO2
1933 kJ
-1875 kJ
3866 kJ
-3750 kJ
The following equations show the oxidation of carbon and carbon monoxide to carbon dioxide.
C(s) +O2(g) → CO2(g) ΔH = –x kJ mol–1
CO(g) + O2(g) → CO2(g) ΔH = –y kJ mol–1
What is the enthalpy change, in kJ mol–1, for the oxidation of carbon to carbon monoxide?
C(s) + O2(g) → CO(g)
x + y
-x - y
y - x
x - y
Identify the incorrect statement about achieving equilibrium.
achieved when product and reactant concentrations are equal
achieved when forward and reverse reaction rates are same
achieved when concentration of reactants is stable/constant
achieved when concentration ratio of reactants to products becomes stable, thus fixing the equilibrium constant (equilibrium position)
Catalysts permit reactions to proceed along a ___________energy path.
lower
higher
magnetic
psycho's
Na2S2O3(aq) + 2HCl(aq) → 2S(s) + SO2(g) + 2NaCl(aq) + H2O(l)
Which list below contains only changes that will decrease the rate of this reaction?
The Maxwell–Boltzmann distribution of molecular energies in a sample of gas at a fixed temperature is shown.
Which letter represents the mean energy of the molecules?
A
B
C
D
The diagram shows the Maxwell−Boltzmann distribution of molecular energies in a gas at two different temperatures.
Which letter represents the most probable energy of the molecules at the higher temperature?
A
B
C
D
The question below is about the Maxwell–Boltzmann distribution shown for a sample of a gas, X, at two different temperatures.
Which statement is correct for the higher temperature?
The area under the curve to the left of Ea decreases.
The total area under the curve increases.
The activation energy decreases.
More molecules have the mean energy.
The graph below shows a typical energy distribution for particles of an ideal gas in a sealed container at a fixed temperature.
Which of the following statements is true?
Position A represents the mean energy of a molecule in the container.
Addition of a catalyst moves the position of EA to the right.
The area under the curve to the right of EA represents the number of molecules with enough energy to react.
The position of the peak of the curve at a higher temperature is further away from both axes.
The total area under the distribution curve represents
total energy.
activation energy.
total number of reacting molecules.
total number of molecules present.
